Midodrine HCl
- Product NDC
- 21695-181
- 11-digit product format
- 216950181
- Labeler code
- 21695
- Product ID
- 21695-181_4a81751e-1c63-4b0d-8f63-bf7c4d155f22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midodrine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA076514
- Marketing category
- ANDA
- Marketing start
- 2002-07-02
- Marketing end
- 0000-00-00
- Substance
- MIDODRINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21695-181-00 | Midodrine HCl | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-181 | MIDODRINE HCL (MIDODRINE HYDROCHLORIDE) TABLET [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 1 package rows | 20110104_4a81751e-1c63-4b0d-8f63-bf7c4d155f22.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-181-00 | 21695018100 | 100 in 1 BOTTLE | Historical |